Diazotrophic Paenibacillus beijingensis BJ-18 Provides Nitrogen for Plant and Promotes Plant Growth, Nitrogen Uptake and Metabolism

Abstract

Diazotrophic bacteria can reduce N₂ into plant-available ammonium (NH₄⁺), promoting plant growth and reducing nitrogen (N) fertilizer requirements. However, there are few systematic studies on the effects of diazotrophic bacteria on biological N₂ fixation (BNF) contribution rate and host plant N uptake and metabolism. In this study, the interactions of the diazotrophic Paenibacillus beijingensis BJ-18 with wheat, maize, and cucumber were investigated when it was inoculated to these plant seedlings grown in both low N and high N soils, with un-inoculated plants as controls. This study showed that GFP-tagged P. beijingensis BJ-18 colonized inside and outside seedlings, forming rhizospheric and endophytic colonies in roots, stems, and leaves. The numbers of this bacterium in the inoculated plants depended on soil N levels. Under low N, inoculation significantly increased shoot dry weight (wheat 86.1%, maize 46.6%, and cucumber 103.6%) and root dry weight (wheat 46.0%, maize 47.5%, and cucumber 20.3%). The ¹⁵N-isotope-enrichment experiment indicated that plant seedlings derived 12.9–36.4% N from BNF. The transcript levels of nifH in the inoculated plants were 0.75–1.61 folds higher in low N soil than those in high N soil. Inoculation enhanced NH₄⁺ and nitrate (NO₃^-) uptake from soil especially under low N. The total N in the inoculated plants were increased by 49.1–92.3% under low N and by 13–15.5% under high N. Inoculation enhanced activities of glutamine synthetase (GS) and nitrate reductase (NR) in plants, especially under low N. The expression levels of N uptake and N metabolism genes: AMT (ammonium transporter), NRT (nitrate transporter), NiR (nitrite reductase), NR, GS and GOGAT (glutamate synthase) in the inoculated plants grown under low N were up-regulated 1.5–91.9 folds, but they were not obviously changed under high N. Taken together, P. beijingensis BJ-18 was an effective, endophytic and diazotrophic bacterium. This bacterium contributed to plants with fixed N₂, promoted plant growth and N uptake, and enhanced gene expression and enzyme activities involved in N uptake and assimilation in plants. However, these positive effects on plants were regulated by soil N status. This study might provide insight into the interactions of plants with beneficial associative and endophytic diazotrophic bacteria.

Introduction

Biological nitrogen (N) fixation (BNF) is the major natural process through which atmospheric N₂ is reduced to bioavailable NH₄⁺, providing a large amount of natural N into cultivated agricultural systems (Galloway et al., 2008). In addition to symbiotic N₂-fixing Rhizobia associated with legumes, the non-symbiotic diazotrophic bacteria are also important contributors to the N nutrition of non-legumes (Gupta et al., 2006). It is estimated that the microbial N accounts for roughly 30–50% of the total N in crop fields (Liu et al., 2017). The non-symbiotic diazotrophic bacteria are highly diverse and associated with plants in different ways. Some bacteria live in the rhizosphere and are designated rhizobacteria (Kloepper and Beauchamp, 1992). Herbaspirilla seropedicae strain Z67 mainly colonize on the riceroot surface and are usually called associative diazotrophic bacteria (Monteiro et al., 2012). Paenibacillus polymyxa WLY78 live inside the plant without causing damage and are classified as endophytic diazotrophic bacteria (Hao and Chen, 2017). Endophytic diazotrophic bacteria may have an advantage over associative diazotrophic bacteria and rhizobacteria, since they live within plant tissues where better niches are established for N₂ fixation and assimilation of fixed N₂ by the plant (Reinhold-Hurek and Hurek, 1998, 2011).

The well-known associative and endophytic diazotrophic bacteria include Azospirillum (Boddey et al., 1986), Azoarcus (Hurek et al., 2002), Burkholderia (Baldani et al., 2000), Enterobacter (Magnani et al., 2010), Gluconacetobacter (James et al., 2001), Herbaspirillum (Boddey et al., 1995). BNF quantification experiments show that associative and endophytic bacteria can fix N₂ in plant tissues with higher efficiency (Carvalho et al., 2014). G. diazotrophicus inoculation enhanced sugarcane yield by providing 50–80% N from BNF (Boddey et al., 1995). It is estimated that an 18–28% of plant N derives from BNF of endophytic Enterobacter sp. strain (Mirza et al., 2001). Diazotrophic bacteria present in the mucilage of aerial roots contribute 29–82% of the N nutrition of Sierra Mixe maize (Van Deynze et al., 2018).

Although the positive effects of diazotrophic bacteria on plants are observed, little is known about plant response to inoculation with diazotrophic bacteria. Plant N metabolism is a complex process requiring some key enzymes. The plant genes NR (nitrate reductase), NiR (nitrite reductase), GS (glutamine synthetase) and GOGAT (glutamate synthase) play very important roles in N metabolism (Bloom et al., 1992; Lea and Miflin, 2003). The plant genes AMT (ammonium transporter) (Bloom et al., 1992) and NRT (nitrate transporter) (Sugiura et al., 2007) are involved in N uptake. It is shown that some endophytic fungi affect expression of N metabolism of plants (Yang et al., 2014).

Paenibacillus beijingensis BJ-18, isolated from wheat rhizosphere, was a N₂-fixer (Wang et al., 2013). Inoculation with P. beijingensis BJ-18 promoted the growth of tomato seedlings (Xie et al., 2016) and increased wheat yield by 26.9% in field experiment (Shi et al., 2016), suggesting that this bacterium promotes plant growth. It was generally recognized that plant growth-promoting bacteria (PGPB) promoted plant growth by direct mechanisms (e.g., N fixation, phosphate solubilization, sequestering iron) and indirect mechanisms [e.g., indole-3-acetic acid (IAA), cytokinins, gibberellins] (Glick, 2012). However, the mechanisms utilized by P. beijingensis BJ-18 to promote plant growth were not clear. In this study, we investigated the colonization pattern and contributions of N₂ fixation by P. beijingensis BJ-18 to plants, and the plant responses (N uptake and metabolism processes) to the infection.

Materials and Methods

Bacteria Strains and Growth Conditions

Paenibacillus beijingensis BJ-18 (accession number: JN873136), isolated from wheat rhizosphere, is a novel species with N₂-fixing ability [1043 ± 12.9 nmol C₂H₄ (mg protein h)^-1] (Wang et al., 2013). This bacterium has multiple antagonistic activities against plant pathogens and produces IAA (24.95 μg mL^-1) (Xie et al., 2016). The bacterial suspension of P. beijingensis BJ-18 used in inoculation was prepared as follows. The P. beijingensis 1–18 cells were cultured overnight in Luria-Bertani (LB) broth at 30°C and 180 rpm, and then cells in the logarithmic growth phase were harvested by centrifugation and finally the pellet was suspended with sterile normal saline (0.89% w/v NaCl in double distilled water) to the final concentration at 10⁸ cells mL^-1.

Colonization of GFP-Tagged P. beijingensis BJ-18 in Wheat, Maize, and Cucumber Tissues

The recombinant plasmid pGFP300 carrying gfp gene (Hao and Chen, 2017) was introduced into P. beijingensis BJ-18 by electrotransformation (Zhang et al., 2013), yielding GFP-tagged P. beijingensis BJ-18. And the physiological ability of GFP-tagged P. beijingensis BJ-18 was not changed, compared with wild-type P. beijingensis BJ-18 (data not published). The GFP-tagged P. beijingensis BJ-18 suspension was obtained as described above. Plump seeds of wheat “Jimai 22” (Shandong Runfeng Seed Industry Co., Ltd), maize “Zhengdan 958” (Henan Shangke Seed Co., Ltd.) and cucumber “Zhongnong 8” (Beijing Shengfeng Garden Agricultural Technology Co., Ltd) were surface-disinfected with 10% sodium hypochlorite for 10 min, followed by rinsing with sterilized water three times, and grown on the sterile petri dishes containing moist filter papers in darkness at room temperature (25°C) for 3–5 days, respectively. These plant seedlings had two treatments: inoculation with GFP-tagged P. beijingensis BJ-18 (E+) and mock inoculation (E-). For inoculation, the plant seedlings were soaked in bacterial suspension (10⁸ cells mL^-1) of GFP-tagged P. beijingensis BJ-18 for 30 min to facilitate colonization. For mock inoculation, the plant seedlings were soaked in sterilized deionized water for 30 min. The germinated wheat, maize and cucumber seeds were, respectively, sown in sterile flask (3 seeds per flask, 6 cm in diameter and 10 cm in height) containing 100 mL 1/2 × Murashige and Skoog semisolid agar medium (Prod No: M519, PhytoTechnology Laboratories, Shawnee Mission, United States) (Murashige and Skoog, 1962). Then these seedlings were grown in the light growth chamber (27°C, 70% humidity and 16 h day/8 h night, with light at 250 μmol m^-2 s^-1). The GFP-tagged P. beijingensis BJ-18 in plant tissues was observed at 2 weeks after inoculation by confocal laser scanning microscopy (CLSM, Olympus FluoView^TM FV1000 confocal microscope, Olympus Corporation, Tokyo, Japan). These images were collected using FV10-ASW software (03.01.02.02, Olympus Europa Holding GmbH, Hamburg Germany) and processed in Adobe Photoshop CC 2015 and Adobe Illustrator CS6 (Adobe, San Jose, CA, United States).

Plant Culture and Collection

Seedling growth assays were performed in plastic pots (diameter of 35 cm; height of 25 cm) filled with 5 kg non-sterile soil which was top soil (0–20 cm depth) taken from the Shangzhuang Experimental Station of China Agricultural University, Beijing, China (40°08′12.15″ N, 116°10′44.83″ E, 50.21 m above sea level). The soil was low N-content sandy loam (N_min, 7.8 mg kg^-1; Olsen-P, 7.3 mg kg^-1; NH₄OAc-K, 115.8 mg kg^-1; O.M., 7.2 g kg^-1; pH 7.7; E.C., 0.4 dS m^-1). The soil was air-dried, crushed, and screened by a 2 mm sieve to remove debris and reduce heterogeneity for cultivating plants: wheat, maize and cucumber. Before planting, P (Na₂HPO₄) and K (KCl) fertilizer were applied to soil as base fertilizers at amounts of 50 mg P and 17 mg K per kg soil, respectively, based on the recommendation by Ke et al. (2018). The microelements were not applied to soil during plant growth.

The experimental design was randomized with factorial arrangement (a 2 × 2 factorial design) in three replications with bacterial factor at two levels and N factor at two levels. Three different plants (wheat, maize, and cucumber) were chosen to obtain an objective conclusion. Therefore, the experiments had twelve treatments.

The seeds (wheat, maize, and cucumber) were germinated as described above. After germination, vigorous and homogenous seedlings were chosen for transplanting into plastic pots. These plant seedlings had two treatments: inoculation with P. beijingensis BJ-18 (E+) and mock inoculation (E-). For inoculation, the plant seedlings were soaked in bacterial suspension (10⁸ cells mL^-1) of P. beijingensis BJ-18 for 30 min to facilitate colonization. For mock inoculation, the plant seedlings were soaked in sterilized deionized water. Then the inoculated seedlings and un-inoculated seedlings were, respectively, transplanted into pots (cucumber: 4 seedlings per pot; maize: 2 seedlings per pot; wheat: 4 hills per pot and 10 seedlings per hill). On day 7, 80 ml of the bacterial suspension was applied to pot containing inoculated seedlings and 80 mL of sterile water was applied to pot containing non-inoculated seedlings. Each of inoculation and mock inoculation treatments had three replicates.

There were two levels of N treatments: high N level (250 mg N kg^-1 soil) and low N level (83 mg N kg^-1 soil). The ¹⁵N-labeled (NH₄)₂SO₄ (10.16% ¹⁵N atom, Shanghai Research Institute of Chemical Industry, China) was applied to soils in all pots. The N fertilizer was added in three separate applications: the first application was done before planting as base fertilizer (approximately 33.3% of total N), and successive two applications (approximately 33.3% of total N per time) were made on day 7 and 14 after transplanting, respectively. Pots were placed in the greenhouse under optimum conditions (15 h light/9 h dark cycle, 25–30/15–20°C day/night temperature and 40% day/60% humidity). The seedlings were regularly watered (tap water) to 40% relative soil moisture by weighing method every 5 days.

The samples of wheat, maize, and cucumber were harvested from each treatment on day 35 after transplanting, respectively.

Firstly, the whole seedling was uprooted, and then shoot and root samples were separated and washed with deionized water to remove the adhering soil. Shoot and root samples were oven-died at 105°C for 30 min to inactivate the enzyme, respectively, followed by 65°C until constant weight for dry weight analysis. Then, the oven-dried samples were grinded, screened by a 1 mm sieve, and stored in zip-lock bag for plant N content and ¹⁵N enrichment determination. Afterward, the remaining samples were immediately frozen in liquid N and then maintained at -80°C until further analysis.

Bacterial Cell Concentration Within Plant Tissues

The cell densities of diazotrophic P. beijingensis BJ-18 within the inoculated plant tissues were estimated by qPCR according to the method described by Rasmussen et al. (2007). Primers for qPCR of the nifB from P. beijingensis BJ-18 included nifB F (5′-GAAGGTGAGAGTGAGGATGG-3′) and nifB R (5′-TTGCTTCAGGCTCATCTCC-3′). qPCR was performed with plant genomic DNA as template which was extracted form plant seedlings using DNA Kit [TianGen Biotech (Beijing) Co., Ltd.]. The 129 bp PCR product was ligated to the PMD 19-T vector (Takara, Otsu, Japan) and then introduced into Escherichia coli JM109. The introduced E. coli JM109 was grown in liquid LB medium, and the recombinant plasmids carrying nifB fragment were extracted and purified using TIANprep Mini Plasmid Kit [TianGen Biotech (Beijing) Co., Ltd.]. A standard curve was generated for each run 10-fold dilution series from 2 × 10¹ to 2 × 10⁷ copies. The plant genomic DNA isolated from each of the different treatments was mixed with SYBR^® Premix Ex TaqTM (Takara, Kyoto, Japan), primer pairs and ddH₂O in a total volume of 20 uL for qPCR on a 7500 Real-Time PCR System (Applied Biosystems, Foster City, CA, United States). Ct values were measured to quantify initial amounts of target DNA.

Quantification of Biological N₂ Fixation Contribution

In this study, BNF contribution of P. beijingensis BJ-18 to plants was quantified by the method of ¹⁵N isotope dilution technique. N content and ¹⁵N enrichment in plant tissues were determined by DELTA V Advantage isotope ratio mass spectrometer (Thermo Fisher Scientific, Inc., United States). The plants without P. beijingensis BJ-18 inoculation were used as references to calculate the BNF contribution. The BNF contribution was calculated according to formula 1 described by Boddey and Knowles (1987):

$$\%\mathrm{Ndfa}=\left(1-\frac{{\%}^{15}\mathrm{Na}.\mathrm{e}{.}_{\mathrm{I}}}{{\%}^{15}\mathrm{Na}.\mathrm{e}{.}_{\mathrm{UI}}}\right)\times 100$$ (1)

Where, %Ndfa is the percentage of N derived from air and percent ¹⁵Na.e. (%¹⁵N atom excess) is the enrichment of the inoculated (I) and un-inoculated (UI) plants, respectively.

Determination of the Concentration of Free NH₄⁺, NO₃^-, and Activities of GS and NR

In order to determine the concentrations of the free ammonium (NH₄⁺) and nitrate (NO₃^-), fresh plant tissues were ground with a mortar on ice in extraction buffer. The buffer consisted of 10 mM imidazole, 50 mM Tris-HCl (pH 8.0), and 0.5% (w/v) β-mercaptoethanol. After grinding, the samples were centrifuged at 12,000 × g for 20 min at 4°C and the supernatant was collected for free NH₄⁺ and NO₃^- determination (Oliveira et al., 2002; Yang et al., 2014). Free NH₄⁺ concentration [μg g^-1 fresh weight (FW)] in the supernatant was assayed using the Berthelot color reaction method (Gordon et al., 1978), and free NO₃^- concentration (μg g^-1 FW) in the supernatant was determined using the Griess method (Eckhardt et al., 1999).

For analysis of GS activity, fresh plant tissues were ground with a mortar in pre-cold extraction buffer (containing10 mM MgSO₄, 2 mM dithiothreitol, 70 mM 3 (n-morpholino) propane-sulfonic acid (pH 6.8), 5 mM glutamate, 10% (v/v) ethanediol, 0.1% (v/v) TritonX-100). The extracts were centrifuged at 12,000 × g for 30 min at 4°C and the supernatant was collected for plant GS activity determination using NH₂OH as a substrate, and the amount of γ-glutamyl hydroxamate (GHA, ug^-1 FW min^-1) released was determined spectrophotometrically at 540 nm according to the method of Yang et al. (2014).

To measure NR activity, fresh plant tissues were ground on ice in extraction buffer consisting of 25 mM phosphate buffer (pH 7.5, a mixture of K₂HPO₄ and KH₂PO₄), 5 mM cysteine and 5 mM EDTA-Na₂. The mixture was centrifuged at 4,000 × g and 4°C for 10 min and the supernatant was collected. NR activity was measured spectrophotometrically at 540 nm according to Yu and Zhang (2012). NR activity was expressed as μg NO₂^- g^-1 FW h^-1.

Quantitative Real-Time PCR Analysis of Plant Genes and nifH in Plant Roots and Shoots

Total RNA was extracted from plant tissues using RNAiso Plus reagent (RaKaRa, Kyoto, Japan). Then, RNA was digested with DNase I and reversely transcribed into cDNA using PrimeScript^TM RT reagent kit (RaKaRa, Kyoto, Japan). Gene expression levels were determined by quantitative real-time PCR (qRT-PCR) analysis. The specific primers for qRT-PCR were shown in Table 1. The plant housekeeping gene actin was used as plant internal control, and the bacterial 16S rRNA was used as bacterium internal control. The relative expression of the target genes were calculated according to the standard comparative C(t) method (Livak and Schmittgen, 2001). Each treatment had three biological replicates, with three technical replicates for each biological replicate.

Table 1.

Primers sequence and accession number in NCBI.

Primer	Primer sequence 5′-3′	Size (bp)	NCBI Accession No.	References
CsAMT1	TTCTCTATCAGTGGGCTTTCG	141	AY642427	This study
	AGAACCAATGGGACACAACC
CsAMT3	AAGGTAGACGACACAATGG	109	XM_004138819	This study
	CGTAGAAGATGTTGTTGAGG
CsNRT 1.3	CACAAGCCTTCAGAGAATTGG	131	JX206800	This study
	TCAACCAGAAAGCACTTATACG
CsNR1	GCACAACTCAGACCAATCC	103	HM755943	This study
	GATGAGAATGCTGTCCATACC
CsNR2	TGTGCGTGTATTCAGATTCG	132	HM755944	This study
	GTGCTAGAGGGCGTATAGG
CsNiR	AGGATTGGTAGCTTGCACTGG	105	EF397679	This study
	ACTGTGACTCGCCGTTGC
CsGS1	ATGAGGGAAGAAGGAGGTTACG	147	JQ277263	This study
	AGAGAAGGTGTGGATGTCAGC
CsGOGAT	GGCTGCTCAAGGAAAGGAACC	127	DQ641082	This study
	TGCTGGATTTGTCACCTGTGC
TaAMT1.1	ACAGCTTCTTCCTCTTCC	105	AY525637	This study
	CCGAGTAGATGAGGTAGG
TaNRT1.1	ATGCCAGGTTGTCATTGC	135	AY587265	This study
	CCGAGTCCAGTTGTATGC
TaNRT2.1	TGGACTCCGAGCACAAGG	104	AF288688	This study
	GACGAAGCAGGTGAAGAAGG
TaNRT2.3	TGGTCAGAGGAGGAGAAGG	101	AY053452	This study
	GTGGCGAGGATAACATTGC
TaNR	ATACACCATGAAAGGATACG	126	KY244026	This study
	TACTTGTTCGGCTTCTCC
TaNiR	CTACACCAACCTCCTCTCC	138	FJ527909	This study
	GCCAGGTCGTTGATATGC
TaGS1	CCTTGTCATGTGCGATTGC	135	DQ124211	This study
	GTGTACTCCTGCTCGATACC
Ta GOGAT	AAACCAAGGGACCTCAGTATTC	150	DW986179	This study
	AATGACCACCACCTTCTTACC
ZmAMT1;1a	CATCGTCGGAAGGTGTGG	109	GRMZM2G175140	This study
	TTGGATGATGAGCAGTGACC
ZmAMT1;1b	CTACGACTTCTTCCTATACC	111	GRMZM2G118950	This study
	CGGAGTAGATGAGGTAGG
ZmNrt2.1	TGGACTCAGAGCACAAGG	102	AY129953	This study
	CGAAGCAGGTGAAGAAGG
ZmNR	GCCAGCATTGAAGGGAAG	106	M77792	This study
	GCTCGTTCTTGAAGTAGACC
ZmGS1-3	CTTGTGATGTGCGATTGC	129	X65928	This study
	CTCCTGCTCAATACCATACC
ZmGS1-4	AGGCATCAACATCAGTGG	117	X65929	This study
	AGAATGTAGCGAGCAACC
Zm GOGAT	CGCTCTTCTGGCAACTGG	133	M59190	This study
	CACCTTCCTGTAGTCTGATTCG
CsACTIN	AGAGATGGCTGGAATAGAAC	333	DQ641117	Wei et al. (2015)
	CTGGTGATGGTGTGAGTC
ZmACTIN	CATGGAGAACTGGCATCACACCTT	118	J01238.1	Galli et al. (2013)
	CTGCGTCATTTTCTCTCTGTTGGC
TaACTIN	GTCGGTGAAGGGGACTTACA	187	AB181991.1	Moloudi et al. (2013)
	TTCATACAGCAGGCAAGCAC
nifB	GAAGGTGAGAGTGAGGATGG	88	MH202771	This study
	TTGCTTCAGGCTCATCTCC
nifH	GCAACAGTCGGAATACGG	136	MH555146	This study
	TTGGGTCACGGTCATACG

Statistical Analysis

Statistical tests were performed using SPSS software version 20 (SPSS Inc., Chicago, IL, United States). Two-way analysis of variance (ANOVA) was employed to check the significant differences between treatments. Means of different treatments were compared using the least significant difference (LSD) at 0.05 or 0.01 level of probability. Graphs were prepared using SigmaPlot software version 12.5 (Systat Software, Inc., CA, United States).

Results

Colonization of GFP-Tagged P. beijingensis BJ-18 in Wheat, Maize, and Cucumber Tissues

The CLSM observation showed that the GFP-tagged P. beijingensis BJ-18 cells emitted bright green fluorescence (Figure 1a). The GFP-tagged P. beijingensis cells were found to colonize on the surface of the primary roots and the root hair zone of wheat (Figure 1b,c). The bacterial cells were found to be distributed within cortex of wheat primary roots (Figure 1d) and colonized in the wheat vascular bundle (Figure 1e). Moreover, bacterial cells were observed in the vascular bundle of wheat stem (Figure 1f,g) and in wheat leaf vein (Figure 1h). In the maize seedlings, the P. beijingensis cells were found to colonize the surface of the primary roots (Figure 2a), and on the junction of the primary and lateral roots (Figure 2b). The bacteria cells were found within the intercellular spaces and xylem vessels of maize roots and stems (Figure 2c–e) and leaves (Figure 2f). The colonization pattern in cucumber was similar to those obtained in wheat and maize seedlings. The bacterial cells were found to colonize the surface of the primary roots and the root hair zone (Figure 3a). The P. beijingensis cells were in cortex (Figure 3b) and vascular bundle (Figure 3c) of cucumber roots. As shown in Figure 3d,e, bacterial cells invaded the xylem vessels of cucumber stem. Moreover, the bacterial cells were found within the cucumber leaves (Figure 3f).

FIGURE 1.

Colonization of the GFP-tagged P. beijingensis BJ-18 in the seedlings of wheat. Wheat seedlings were grown in the presence of GFP-tagged P. beijingensis BJ-18 for 2 weeks. Images were taken with a fluorescent microscope. Excitation was at 488 nm. (a) Confocal image of the GFP-tagged P. beijingensis BJ-18 cells; (b–e) Colonization patterns in the root; (f,g) Colonization patterns in the stem; (h) Colonization patterns in the leaf. Bars represent 50 μm.

FIGURE 2.

Colonization of the GFP-tagged P. beijingensis BJ-18 in the seedlings of maize. Maize seedlings were grown in the presence of GFP-tagged P. beijingensis BJ-18 for 2 weeks. Images were taken with a fluorescent microscope. (a–c) Colonization patterns in the root; (d,e) Colonization patterns in the stem; (f) Colonization patterns in the leaf. Bars represent 50 μm.

FIGURE 3.

Colonization of the GFP-tagged P. beijingensis BJ-18 in the seedlings of cucumber. Cucumber seedlings were grown in the presence of GFP-tagged P. beijingensis BJ-18 for 2 weeks. Images were taken with a fluorescent microscope. (a–d) Colonization patterns in the root; (e) Colonization patterns in the stem; (f) Colonization patterns in the leaf. Bars represent 50 μm.

Taken together, P. beijingensis cells colonized on the surface of roots and within roots, stems and leaves of wheat, maize, and cucumber, indicating that the colonization patterns in the three plants were similar.

Concentration of Diazotrophic P. beijingensis BJ-18 in Wheat, Maize, and Cucumber Tissues

The concentration of P. beijingensis BJ-18 in the inoculated plants at 35 day after inoculation was assessed using qPCR and was expressed as the number of copies of the specific nifB genes per total (plant seedlings + bacteria) genomic DNA. As shown in Figure 4, copy numbers of nifB gene in the inoculated plant tissues under low N level were much higher than under high N level. Wheat had the highest copy numbers of P. beijingensis nifB gene, followed by cucumber and then maize under both low N and high N levels. Copy numbers of nifB gene in roots of the three plants were much higher (62.5–185.3%) than in shoots under both low N and high N levels. These data suggested that the concentrations of the bacterial cells in plant tissues were related to soil N levels, plant species and plant tissues.

FIGURE 4.

The cell concentrations of P. beijingensis BJ-18 in the inoculated shoots and roots of wheat, maize, and cucumber seedlings in high N (HN) and low N (LN) levels. The concentrations of P. beijingensis BJ-18 are represented by nifB gene copies ng^-1 total genomic DNA. Values are given as mean of three independent biological replicates, and single asterisks or double asterisks (^∗ or ^∗∗) indicate significant differences between HNE+ and LNE+ treatments determined by LSD at P < 0.05 or P < 0.01. The bars represent the standard error. LNE+ indicates plants grown in low N level of soils and inoculated with P. beijingensis BJ-18; HNE+ indicates plants grown in high N level of soils and inoculated with P. beijingensis BJ-18.

Plant Growth Promotion

To assess the impacts of P. beijingensis inoculation on plant growth, the biomass (dry weight) was analyzed in inoculated and un-inoculated plants under low N and high N levels. Dry weights of wheat shoots and in roots under low N were increased by 86.1 and 46.0%, respectively. Dry weights of maize shoots and in roots under low N were increased by 46.6 and 47.5%, respectively. Dry weights of cucumber shoots and in roots under low N were increased by 103.6 and 20.3%, respectively. The data suggested that P. beijingensis BJ-18 could efficiently promote the growth of the three plants (Figure 5). The increased shoot and root biomass by P. beijingensis BJ-18 inoculation under low N condition were significantly higher than those under high N condition, consistent with the concentration of P. beijingensis BJ-18 in these plant tissues under different N conditions.

FIGURE 5.

Dry weight (DW) in shoots (A) and roots (B) of wheat, maize, and cucumber seedlings inoculated with P. beijingensis BJ-18 under high N (HN) and low N (LN) levels. Values are given as mean of three independent biological replicates, and single asterisks or double asterisks (^∗ or ^∗∗) indicate significant differences between inoculated (E+) and un-inoculated (E-) plants determined by LSD at P < 0.05 or P < 0.01. The bars represent the standard error. The wheat dry weight represents five seedlings per pot, and the dry weight of maize and cucumber represents one seedling per pot. LNE- indicates plants grown in low N level of soil and un-inoculated with P. beijingensis BJ-18; LNE+ indicates plants grown in low N level of soils and inoculated with P. beijingensis BJ-18; HNE- indicates plants grown in high N level of soil and un-inoculated with P. beijingensis BJ-18; HNE+ indicates plants grown in high N level of soils and inoculated with P. beijingensis BJ-18.

Quantification of BNF in the P. beijingensis-Inoculated Wheat, Maize, and Cucumber

To estimate the contribution of BNF, ¹⁵N isotope enrichment analysis was conducted to analyze inoculated seedling of wheat, maize and cucumber grown in soil contain ¹⁵N-labeled (NH₄)₂SO₄ as N fertilizer in greenhouse conditions, in comparison with un-inoculated plants. As shown in Table 2, the roots and shoots of seedlings inoculated with P. beijingensis BJ-18 had significantly lower δ¹⁵N value than un-inoculated seedlings under both low and high N conditions, suggesting that these plants derived a portion of N from atmospheric N₂. The plant N derived from the atmosphere (%Ndfa) ranged from 18 to 36.4% under low N level and from 12.9 to 30.5% under high N level. Among the three plants, wheat showed maximum %Ndfa (30.5 and 36.4%) under both high N and low N levels, followed by cucumber (25.4 and 27.8%) and then maize (12.9 and 20.9%). These data suggest that the contribution of BNF was closely related to soil N levels and to plant species. These results were in agreement with the concentration of P. beijingensis BJ-18 within plants and the plant biomass under different N levels.

Table 2.

¹⁵N isotope enrichment determination of biological N₂ fixation rate in inoculated plants grown in soils containing high N and low N.

Treatments			δ15N value (versus at-air)		%Ndfa
			High N	Low N	High N	Low N
	Shoot	E-		10952 ± 1251a	3680 ± 261a
Cucumber		E+	7641 ± 727a	2656 ± 176b	25.4 ± 0.4b	27.8 ± 0.4a
	Root	E-	12926 ± 443a	4282 ± 738a	—	—
		E+	9457 ± 197b	2935 ± 503b	26.8 ± 1.1b	31.4 ± 0.9a
	Shoot	E-	6662 ± 1076a	3056 ± 299a	—	—
Wheat		E+	4596 ± 631a	1940 ± 171b	30.5 ± 1.8b	36.4 ± 0.6a
	Root	E-	6123 ± 316a	3573 ± 234a	—	—
		E+	4758 ± 274b	2614 ± 172b	22.3 ± 0.9b	26.9 ± 0.4a
	Shoot	E-	5383 ± 434a	2222 ± 137a	—	—
Maize		E+	4677 ± 296a	1756 ± 88b	12.9 ± 1.5b	20.9 ± 1.0a
	Root	E-	4523 ± 174a	2357 ± 292a	—	—
		E+	3885 ± 160a	1932 ± 235b	14.1 ± 0.4b	18.0 ± 0.3a

Values are given as mean ± SE of three independent biological replicates. Different letters indicates indicate significantly differences in δ15N value inoculated (E+) and un-inoculated (E-) plants according to the LSD test (P < 0.05); Different letters indicate significantly differences in %Ndfa between high N and low N according to the LSD test (P < 0.05); δ¹⁵N value: percent atom excess ¹⁵N; %Ndfa: percent N derived from atmosphere.

Transcript Levels of nifH Gene

To investigate whether nif genes coding nitrogenase of P. beijingensis BJ-18 were expressed within plant tissues, the transcript levels of nifH gene, one of nif genes coding Fe protein of nitrogenase, were quantified. As shown in Figure 6, transcripts of nifH under low N were up-regulated in wheat shoots and roots by 1.09 and 1.61 folds, respectively, in maize shoots and roots by 0.77 and 1.0 folds, respectively, and in cucumber shoots and roots by 0.75 and 1.61 folds, respectively, compared to those under high N. The results suggested that soil N status affected transcript level of P. beijingensis nifH. The data were consistent with BNF rate and the concentration of P. beijingensis BJ-18 in plants grown in soils containing different N levels.

FIGURE 6.

The nifH transcript levels of P. beijingensis BJ-18 in shoots and roots of wheat, maize and cucumber seedlings inoculated with P. beijingensis BJ-18 under high N (HN) and low N (LN) levels. Values are given as mean of three independent biological replicates, and single asterisks or double asterisks (^∗ or ^∗∗) indicate significant differences between HNE+ and LNE+ treatments determined by LSD at P < 0.05 or P < 0.01. The bars represent the standard error. LNE+ indicates plants grown in low N level of soils and inoculated with P. beijingensis BJ-18; HNE+ indicates plants grown in high N level of soils and inoculated with P. beijingensis BJ-18.

Promotion of N Uptake and Total N Content in Plants by Inoculation With P. beijingensis BJ-18

Compared to un-inoculated shoots and roots under low N level, a significant increase of free NH₄⁺ concentration was observed in shoots of wheat (26.6%), maize (21.9%) and cucumber (22.2%) and in roots of wheat (24.9%), maize (52.7%) and cucumber (32.2%) (Figure 7A). In contrast, inoculation did not significantly enhance free NH₄⁺ concentration in plant tissues under high N (Figure 7B).

FIGURE 7.

Ammonium (NH₄⁺) (A: shoot; B: root), nitrate (NO₃^-) (C: shoot; D: root) and total N (E: shoot; F: root) content in shoots and roots of wheat, maize and cucumber seedlings inoculated with P. beijingensis BJ-18 under high N (HN) and low N (LN) levels. Values are given as mean of three independent biological replicates, and single asterisks or double asterisks (^∗ or ^∗∗) indicate significant differences between inoculated (E+) and un-inoculated (E-) plants determined by LSD at P < 0.05 or P < 0.01. The bars represent the standard error. LNE- indicates plants grown in low N level of soil and un-inoculated with P. beijingensis BJ-18; LNE+ indicates plants grown in low N level of soils and inoculated with P. beijingensis BJ-18; HNE- indicates plants grown in high N level of soil and un-inoculated with P. beijingensis BJ-18; HNE+ indicates plants grown in high N level of soils and inoculated with P. beijingensis BJ-18.

Similarly, P. beijingensis inoculation significantly increased the free NO₃^- concentration in shoots of wheat (26.3%), maize (23.4%) and cucumber (43.7%) and in roots of wheat (60.7%), maize (62.6%) and cucumber (67.4%) under low N (Figure 7C). In contrast, inoculation did not significantly enhance free NO₃^- concentration in plant tissues under high N (Figure 7D).

Compared to un-inoculated shoots under low N level, a significant increase of total N content was observed in inoculated shoots of wheat (76.3%), maize (49.1%) and cucumber (88.8%) (Figure 7E). Similarly, inoculation greatly enhanced total N content in inoculated roots of wheat (61.6%), maize (68.9%) and cucumber (92.3%) (Figure 7F). In contrast, the increased levels of total N content in root and shoots were lower under high N (Figure 7E,F). The data were consistent with the change of the concentrations of the free NH₄⁺, and free NO₃^- under low N and high N.

Enhancement of GS and NR Activities of Plants by Inoculation With P. beijingensis 1-18

Compared to un-inoculated plant shoots and roots under low N (Figure 8A,B), GS activities were significantly increased in inoculated shoots of wheat (89.7%), maize (19.0%) and cucumber (46.9%) and in inoculated roots of wheat (45.0%), maize (85.5%) and cucumber (40.4%), but inoculation did not obviously enhance the GS activities of plants grown in high N soil.

FIGURE 8.

Glutamine synthetase (GS) (A: shoot; B: root) and Nitrate reductase (NR) (C: shoot; D: root) activities in shoots and roots of wheat, maize, and cucumber seedling inoculated with P. beijingensis BJ-18 under high N (HN) and low (LN) levels. Values are given as mean of three independent biological replicates, and single asterisks or double asterisks (^∗ or ^∗∗) indicate significant differences between inoculated (E+) and un-inoculated (E-) plants determined by LSD at P < 0.05 or P < 0.01. The bars represent the standard error. LNE- indicates plants grown in low N level of soil and un-inoculated with P. beijingensis BJ-18; LNE+ indicates plants grown in low N level of soils and inoculated with P. beijingensis BJ-18; HNE- indicates plants grown in high N level of soil and un-inoculated with P. beijingensis BJ-18; HNE+ indicates plants grown in high N level of soils and inoculated with P. beijingensis BJ-18.

As shown in Figure 8C,D, compared to un-inoculated plant shoots and roots grown in low N soil, NR activities were significantly enhanced in inoculated shoots of wheat (20.9%), maize (42.0%) and cucumber (28.9%) and in inoculated roots of wheat (28.9%), maize (66.2%) and cucumber (44.3%). In contrast, inoculation did not obviously enhance the NR activities of plants grown in high N soil.

Up-Regulation of Expression of N Uptake and N Assimilation Genes in Plants by Inoculation With P. beijingensis

In maize, the transcript levels of three genes (ZmAMT1,1a, ZmAMT1,1b, and ZmNRT2.1) involved in N uptake and five genes (ZmNR, ZmNiR, ZmGS1-3, ZmGS1-4, and Zm CsGOGAT) involved N metabolism were analyzed (Figure 9). Under low N level, the transcript levels of ZmAMT1,1a, ZmAMT1,1b, and ZmNRT2.1 were up-regulated by 1.83–3.93 folds in the inoculated shoots, while in inoculated roots, they were up-regulated 2.97–14.17 folds (Figure 9A–C), suggesting that inoculation promoted expression of plant N uptake genes. Similarly, inoculation significantly enhanced the transcript levels of ZmNR, ZmGS1-3, and ZmGS1-4 in shoots by 18.46, 7.44, and 11.79 folds, respectively, and in roots by 5.63, 6.64, and 6.59 folds, respectively (Figure 9D,F,G). In contrast, inoculation did not obviously affect the transcript levels of these genes in maize shoots and roots under high N condition. However, inoculation did not affect the transcript levels of ZmNiR and ZmGOGAT under both low N and high N conditions (Figure 9E,H).

FIGURE 9.

The transcript levels of genes involved N uptake (A: ZmAMT1, 1a; B: ZmAMT1, 1b; C: Zm NRT2.1) and assimilation (D: ZmNR; E: ZmNiR; F: ZmGS1-3; G: ZmGS-4; H: ZmGOGAT) in shoots and roots of maize seedlings inoculated with P. beijingensis BJ-18 under high N (HN) and low N (LN) levels. Values are given as mean of three independent biological replicates, and single asterisks or double asterisks (^∗ or ^∗∗) indicate significant differences between inoculated (E+) and un-inoculated (E-) plants determined by LSD at P < 0.05 or P < 0.01. The bars represent the standard error. LNE- indicates plants grown in low N level of soil and un-inoculated with P. beijingensis BJ-18; LNE+ indicates plants grown in low N level of soils and inoculated with P. beijingensis BJ-18; HNE- indicates plants grown in high N level of soil and un-inoculated with P. beijingensis BJ-18; HNE+ indicates plants grown in high N level of soils and inoculated with P. beijingensis BJ-18.

In wheat, the transcript levels of four genes (TaAMT1.1, TaNRT1.1, TaNRT2.1, and TaNRT2.3) involved in N uptake and four genes (TaNR, TaNiR, TaGS1, and TaGOGAT) involved N metabolism were analyzed. Similar to maize, the eight genes in the inoculated shoots of wheat in low N were up-regulated by 1.56–46.49 folds, while they were up-regulated 1.98–91.93 folds in inoculated roots (Figure 10). In contrast, inoculation did not obviously affect the transcript levels of these genes under high N condition.

FIGURE 10.

Transcript levels of genes involved N uptake (A: TaAMT1.1; B: TaNRT1.1; C: TaNRT2.1; D: TaNRT2.3) and assimilation (E: TaNR; F: TaNiR; G: TaGS1; H: TaGOGAT) in shoots and roots of wheat seedlings inoculated with P. beijingensis BJ-18 under high N (HN) and low N (LN) levels. Values are given as mean of three independent biological replicates, and single asterisks or double asterisks (^∗ or ^∗∗) indicate significant differences between inoculated (E+) and un-inoculated (E-) plants determined by LSD at P < 0.05 or P < 0.01. The bars represent the standard error. LNE- indicates plants grown in low N level of soil and un-inoculated with P. beijingensis BJ-18; LNE+ indicates plants grown in low N level of soils and inoculated with P. beijingensis BJ-18; HNE- indicates plants grown in high N level of soil and un-inoculated with P. beijingensis BJ-18; HNE+ indicates plants grown in high N level of soils and inoculated with P. beijingensis BJ-18.

In cucumber, the transcript levels of four genes (CsAMT1, CsAMT3, CsNRT1.3, and CsNRT2.2) involved in N uptake and five genes (CsNR1, CsNR2, CsNiR, CsGS1, and CsGOGAT) involved N metabolism were also analyzed. Similar to wheat and maize, the nine genes in the inoculated shoots of cucumber in low N soil were up-regulated 1.60–5.82 folds, while they were up-regulated 1.47–11.85 folds in inoculated roots (Figure 11). However, these effects of inoculated were weak when cucumber was grown in high N soil.

FIGURE 11.

The transcript levels of genes involved N uptake (A: CsAMT1; B: CsAMT3; C: CsNRT1.3; D: CsNRT2.2) and assimilation (E: CsNR1; F: CsNR2; G: CsNiR; H: CsGS1; I: CsGOGAT) in shoots and roots of cucumber seedlings inoculated with P. beijingensis BJ-18 under high N (HN) and low N (LN) levels. Values are given as mean of three independent biological replicates, and single asterisks or double asterisks (^∗ or ^∗∗) indicate significant differences between inoculated (E+) and un-inoculated (E-) plants determined by LSD at P < 0.05 or P < 0.01. The bars represent the standard error. LNE- indicates plants grown in low N level of soil and un-inoculated with P. beijingensis BJ-18; LNE+ indicates plants grown in low N level of soils and inoculated with P. beijingensis BJ-18; HNE- indicates plants grown in high N level of soil and un-inoculated with P. beijingensis BJ-18; HNE+ indicates plants grown in high N level of soils and inoculated with P. beijingensis BJ-18.

Discussion

The N₂-fixing Paenibacillus strains have gained much attention due to their capacity of forming endospore to survive for long periods of time under adverse conditions (Grady et al., 2016). In this study, P. beijingensis BJ-18 was tagged by GFP and observation by laser confocal microscopy revealed that in seedlings of wheat, maize, and cucumber, bacterial cells could be found in the inner cortex and vascular bundle of roots and stems as well as within the leaves, suggesting P. beijingensis BJ-18 has similar invasion patterns in both monocotyledons and dicotyledons. The data indicated that P. beijingensis BJ-18 spread systemically from roots to stems and leaves of wheat, maize, and cucumber via xylem vessels. Therefore, P. beijingensis BJ-18 could be defined as a plant endophytic diazotrophic bacterium and it had a broad range of host plants. Similar colonization patterns were observed in the association of P. polymyxa WLY78 with wheat, maize, and cucumber (Hao and Chen, 2017) and in the association of P. polymyxa P2b-2R with lodgepole pine (a gymnosperm tree species) (Anand and Chanway, 2013). The colonization pattern of P. beijingensis BJ-18 was a little different form that of the associated diazotrophic A. brasilense Yu62 which colonized mainly on the surface of maize roots and only small part entered into maize tissues (Liu et al., 2003). These results indicated that on one side the diazotrophic Paenibacillus species/strains may fix N₂ inside plants and rapidly transfer the fixed product to plants, and on the other side they fix N₂ on the root surfaces and part of the fixed product may be remain in the soil.

In this study, the concentrations of P. beijingensis cells in inoculated plant tissues under high N and low N levels were determined by qPCR, with un-inoculated plant tissues as control. The results showed that the bacterial cell numbers were significantly higher in inoculated plant tissues grown under low N condition than those under high N condition, suggesting that soil N status controlled the concentration of bacterial cells in plants. Similar reports were found in sugarcane where high dose of N (ammonium nitrate) resulted in reduction of endophytic Acetobacter diazotrophicus concentration (Fuentes-Ramirez et al., 1999) and a higher number of endophytic diazotrophs were isolated from sugarcane plants under low N than under high N (de Oliveira et al., 2003). Moreover, it was reported that the plant endogenous N status could also induce plant defense responses to regulate bacterial colonization (Carvalho et al., 2014). The increase in N compounds and amino acids (such as phenylalanine and hydroxyproline) was necessary to activate plant defense responses (Snoeijers et al., 2000). Amino acid transporters regulated by N status also have regulatory function in plant defense responses (Liu et al., 2010; Seifi et al., 2013). This study also showed that total N content and concentrations of NH₄⁺ and NO₃^- in un-inoculated plants under high N were much higher than those under low N. This finding may explain why high N caused a decrease in the numbers of P. beijingensis cells in plants tissues.

Furthermore, this study investigated whether nifH gene was expressed in the inoculated plants. The expression levels of nifH in the inoculated plant shoots and roots under low N were significantly higher than those under high N, consistent with the concentrations of P. beijingensis cells. It was well known that nif gene expression was inhibited by high concentrations of NH₄⁺ (Dixon and Kahn, 2004). GlnR mediated positive and negative regulation of nif gene expression in P. polymyxa WLY78 according to N availably (Wang et al., 2018). As mentioned above, there were high concentrations of NH₄⁺ in plants under high N. Thus, P. beijingensis cells in plant tissues sensed the N signal and then regulated nifH expression according to change of N levels. The expression of nif gene of Herbaspirillum seropedicae in maize, sorghum, wheat, and rice plants was reported (Roncato-Maccari et al., 2003). Similar report was found that N fertilizer application inhibited nifH gene expression of the endophytic diazotroph in sugarcane leaves (Jia Hui et al., 2017).

An important metric to evaluate the role of diazotrophic bacteria is whether they can provide fixed N₂ to the host plant. The ¹⁵N isotope dilution analysis has been widely applied to quantify BNF in non-legume plant species such as rice inoculated with Herbaspirillum seropedicae Z67 (James et al., 2002), wheat with Azospirillum brasilense Wa5 (Christiansenweniger and Vanveen, 1991), Kallar grass with Azoarcus sp. BH72 (Hurek et al., 2002) and maize with P. polymyxa P2b-2R (Puri et al., 2015). Here, ¹⁵N isotope enrichment analysis method was used to estimate the contribution of BNF by P. beijingensis BJ-18 inoculation to plants. The BNF rates in the three different plants were higher under low N level than under high N level, indicating that BNF was affected by N levels. The data were consistent with the nif gene expression and the concentrations of P. beijingensis BJ-18 within the plant tissues under different N levels. Similar results were reported that sugarcane plants inoculated with diazotrophic strains gained higher N from BNF in the N-deficient soil (de Oliveira et al., 2003). This study also revealed that wheat gained the highest N from BNF under both low N and high N levels, followed by cucumber and then by maize, suggesting that BNF rate was related to host plant species. The shoots and roots of palm inoculated with Bacillus sphaericus UPMB-10 gained 13.2–13.4% N from BNF (Zakry et al., 2012), which was lower than that gained by inoculation with P. beijingensis BJ-18.

In this study, the effects of P. beijingensis BJ-18 inoculation on plant N uptake and metabolism were investigated. The concentrations of NO₃^-, NH₄⁺ and total N were higher in roots and shoots of inoculated plants than in un-inoculated plants, and were higher in roots than in shoots. The positive effects were also controlled by soil N status. The results indicated that inoculation with P. beijingensis BJ-18 promoted plants to uptake NO₃^- and NH₄⁺ from soil. The increased concentrations of NH₄⁺ and total N in inoculated plants were at least partially resulted from BNF. Studies on the effects of diazotrophs on plant N uptake and metabolism were rare. However, inoculations with some endophytic fungi significantly improved N accumulation and metabolism were observed in rice (Yang et al., 2014), sugar beet (Shi et al., 2009), and tall fescue (Lyons et al., 1990).

NO₃^- was mainly absorbed via NRT protein family members, and then transformed into NH₄⁺ by NR. In this study, P. beijingensis BJ-18-inoculated plants showed significantly higher expression levels of NRT genes (CsNRT1.3 and CsNRT2.2 in cucumber; TaNRT1.1, TaNRT2.1, and TaNRT2.3 in wheat; ZmNRT2.1 in maize) in both shoots and roots under low N condition. Similar reports were found that under low N condition NRT genes were significantly up-regulated in rice inoculated with endophytic fungus Phomopsis liquidambari (Yang et al., 2014) and in tomato inoculated with diazotrophic Enterobacter radicincitans (Berger et al., 2013).

Higher NR activities were observed in the P. beijingensis BJ-18-inoculated plants. It was reported that inoculation with endophytic fungus Plectosphaerella cucumerina F11 greatly increased the activity of NR in sugar beet (Shi et al., 2009). To investigate whether the changes of NR activities in the P. beijingensis BJ-18- inoculated plants were closely related to differential expression of plant NR genes, the expression levels of NR genes were quantified. qRT-PCR analysis indicated that the expression levels of NR genes (CsNR2 in cucumber, TaNR in wheat and ZmNR in maize) were significantly higher in inoculated plants than in un-inoculated plants under low N. It was reported that the endophytic fungus Piriformospora indica inoculation promoted N accumulation in Arabidopsis and tobacco seedlings by inducing the expression of NR (Sherameti et al., 2005). In contrast, endophytic fungus Phomopsis liquidambari inoculation significantly reduced NO₃^- concentration in rice shoots under low N condition, since the higher NR activity made more NO₃^- to be transformed into NH₄⁺ (Yang et al., 2014).

This study demonstrated that P. beijingensis BJ-18-inoculated plants showed higher NH₄⁺ concentration in roots and shoots, compared with those in un-inoculated plants. NH₄⁺ was absorbed via AMT protein family members mainly, and then transformed into organic molecules by GS and GOGAT. GS is an important rate-limiting enzyme in NH₄⁺ assimilation. The higher GS activities were observed in the P. beijingensis BJ-18-inoculated plants than those in un-inoculated plants. GS activities were closely related to soil N status. Transcript levels of GS genes were also measured to confirm whether the changes of GS activities in plants caused by P. beijingensis BJ-18 inoculation were related to GS genes transcription. qRT-PCR indicated that the higher expression levels of GS genes (CsGS1, TaGS1, ZmGS1-3, and ZmGS1-4) in inoculated plant tissues than in un-inoculated ones under low N. Similarly, it was also reported that the expression levels of GS genes were also significantly higher in inoculated plants with the endophytic fungus P. liquidambari than in un-inoculated plants under low N (Yang et al., 2014).

This study demonstrated that inoculation with P. beijingensis BJ-18 promoted dry weight of plant roots and shoots grown under low N to be increased by 20.3–103.6%. The current results were in agreement with previous reports that inoculation with P. beijingensis BJ-18 increased wheat yield by 26.9% in field experiment (Shi et al., 2016) and increased tomato shoot length, fresh weight, and dry weight in the pot experiments (Xie et al., 2016).

The plant-growth-promoting rhizobacteria facilitate plant growth by several direct and indirect mechanisms. Direct mechanisms include P solubilization, N fixation and hormone (e.g., IAA, cytokinins and gibberellins) production. Indirect mechanisms include controlling phytopathogens by producing antibiotics or lytic enzymes (Glick, 2012). As mentioned above, P. beijingensis BJ-18 provided N for plants by BNF and thus promoted plant growth. Also, this bacterium may promote plant growth by producing IAA and antimicrobial compounds (Xie et al., 2016). Compared to A. brasilense Yu62 which produced high amount of IAA, P. beijingensis BJ-18 produced a little amount of IAA. Thus, IAA produced by P. beijingensis BJ-18 might be not the major factor promoting plant growth. Since the soil used in greenhouse study was not sterile, the BNF/plant growth promotion observed in this study could have been in part due to one or several indigenous microbes present in that soil. This study for the first time revealed that P. beijingensis BJ-18 promoted plants to uptake N from soil and enhanced gene expression and enzyme activities involved in N uptake and assimilation in plants. In addition to BNF, these endogenous changes in plants induced by P. beijingensis BJ-18 might be another major factor promoting plant growth.

Conclusion

This study demonstrated that P. beijingensis BJ-18 was an effective and endophytic diazotrophic bacterium which has similar colonization patterns in monocotylous and dicotyledonous plants. This bacterium promoted plant growth by direct mechanisms through BNF. Also, this bacterium might promote plant growth by indirect mechanisms through inducing endogenous changes in plants, including enhancement of N uptake and enzyme activities, and expression of N uptake and assimilation genes. The bacterial density within plant was closely related to the BNF efficiency and the endogenous changes in plants. However, the bacterial density, the BNF efficiency and the endogenous changes in plants during the association with P. beijingensis BJ-18 were controlled by the soil N status. These data suggested that successful colonization of P. beijingensis BJ-18 on plant was the first key step for this bacterium to promote plant growth by BNF and by inducing endogenous changes in plants. How soil N level affects bacterial colonization deserves further study.

Author Contributions

YbL and SC designed and wrote the manuscript. YbL, YlL, HZ, and MW conducted the experiments.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.